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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/SCDO_0000303"/>
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    <!-- http://purl.obolibrary.org/obo/SCDO_0000391 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/SCDO_0000391">
        <rdfs:label>Disease Modifier</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/SCDO_0001000"/>
        <ns2:SCDO_0000303>These article contains a recent description of disease modifiers for SCD: http://www.nejm.org/doi/10.1056/NEJMra1510865 -- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562292/ --  -- Paper mentioning haplotypes and severity: -- https://www.nature.com/scitable/topicpage/sickle-cell-anemia-a-look-at-global-8756219 --  -- Initially, the HP term &quot;Clinical Modifier&quot; (HP:0012823) was used to define this class, but its usage was found to be more &quot;ontology-based&quot; than what the SCDO intended.</ns2:SCDO_0000303>
        <ns2:SCDO_1000288>None</ns2:SCDO_1000288>
        <dc:creator>SCDO (Jade Hotchkiss)</dc:creator>
        <ns2:IAO_0000115>A factor that modifies one or more aspects of a disease, such as sickle cell disease (SCD) (e.g. aspects such as temporal pattern, age of onset and mortality), for specific phenotype(s) of the disease.</ns2:IAO_0000115>
        <oboInOwl:hasExactSynonym>Phenotypic Modifier</oboInOwl:hasExactSynonym>
        <ns2:SCDO_0000303>Request inclusion into relevant ontology</ns2:SCDO_0000303>
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    <!-- http://purl.obolibrary.org/obo/SCDO_0001000 -->

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